Research: Results MTBVAC vaccine candidate offer hope for control of tuberculosis in infants
Results from new trial of the candidate TB vaccine MTBVAC offer hope for control of tuberculosis in infants Press release: Results from new trial of the candidate TB vaccine MTBVAC offer hope for control of tuberculosis in infants
First trial of a new live attenuated Mycobacterium tuberculosis vaccine in infants
Cape Town/Porriño/Zaragoza/Lelystad:
The South African Tuberculosis Vaccine Initiative (SATVI), Biofabri, the University of Zaragoza and TuBerculosis Vaccine Initiative (TBVI) announced promising new safety and immunogenicity results for the live, attenuated Mycobacterium tuberculosis vaccine MTBVAC in BCG-naive South African infants, appearing online in The Lancet Respiratory Medicine on 12 Aug 2019.
This Phase 1b study, conducted in a TB endemic community, showed that vaccination of infants with MTBVAC displayed a similar safety profile and had indistinguishable reactions at the injection site to that of the current licensed TB vaccine, Bacille Calmette-Guérin (BCG), which has an excellent safety record. Vaccination with MTBVAC induced a long-lasting immune response of greater magnitude than that of BCG at a comparable dose. These promising data support further progression of MTBVAC through ongoing Phase 2a dose-defining studies and into large-scale infant efficacy trials.
MTBVAC was also shown to induce dose-dependent conversion and in some cases reversion of the QuantiFERON test (QFT), a diagnostic tool originally designed to detect infection with M. tuberculosis. This is not surprising since MTBVAC is a live, attenuated M. tuberculosis vaccine. In fact, these outcomes may be seen as an encouraging sign of stimulating immune responses against M. tuberculosis, but represent a challenge to interpretation of QFT results in MTBVAC recipients. Ongoing Phase 2a and future efficacy studies in TB endemic countries will allow more extensive evaluation of QFT dynamics in infants, and encourage development of new diagnostic tests to differentiate the MTBVAC-induced response from natural M. tuberculosis infection.
These exciting results are an important step towards a more effective TB vaccine- Professor Mark Hatherill
Positive assessment of results
Professor Mark Hatherill, SATVI Director: “These exciting results are an important step towards a more effective TB vaccine, and support plans for a much larger trial to better define the safety and efficacy of MTBVAC in infants living in TB endemic countries.”
The encouraging results from this trial show that MTBVAC is capable of inducing robust and durable immune responses, Prof Tom Scriba.
Professor Tom Scriba, SATVI Deputy Director, Immunology: “The encouraging results from this trial show that MTBVAC is capable of inducing robust and durable immune responses and trigger the next stage of evaluation for this vaccine candidate. “
Esteban Rodríguez General Manager of Biofabri: In 2008, Biofabri acquired the commitment to make available MTBVAC vaccine worldwide and at an affordable price. Such a commitment enhances Biofabri's involvement in the fight against tuberculosis disease, particularly in low income countries.
Carlos Martin of University of Zaragoza: The next step is to demonstrate the efficacy of MTBVAC in tuberculosis endemic countries. The sooner we can show the efficacy of MTBVAC in clinical trials, the earlier MTBVAC could help us save millions of lives.
Jelle Thole of TBVI: A new vaccine against tuberculosis is urgently needed for all age groups. It is therefore very encouraging to see these promising results for a new vaccine that offers hope for a better vaccine that can be delivered to infants.
About the partners
For media enquiries:
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Biofabri: Esteban Rodríguez, Director General , email: Beatriz Díaz Lorenzo
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University of Zaragoza, Professor Carlos Martin, Professor of Microbiology Email: Carmina Puyod
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South African Tuberculosis Vaccine Initiative (SATVI), UCT, Professor Mark Hatherill Email: Kelvin Vollenhoven